Nina Ishorst

Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate

Elisabeth Mangold, Anne C. Böhmer, Nina Ishorst et al. · The American Journal of Human Genetics · 2016 · 102 citations · Full text

Developmental Anomaly, Developmental Biology, Genetic Disorder +10

Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis

Charlotte W. Ockeloen, Kriti D. Khandelwal, K Dreesen et al. · Genetics in Medicine · 2016 · 79 citations · Full text

Odontology, Developmental Biology, Signal Transduction +9

LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding

Kerstin U. Ludwig, Ricarda Maria Schmithausen, David Li et al. · Nature Biotechnology · 2021 · 77 citations · Full text

Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing

Ann‐Kathrin Hoebel, Dmitriy Drichel, Micha van de Vorst et al. · Journal of Dental Research · 2017 · 39 citations

Genetics, Genetic Epidemiology, Pathology +25

Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene

Iris A.L.M. van Rooij, Kerstin U. Ludwig, Julia Welzenbach et al. · Genes · 2019 · 32 citations · Full text